Oxycodone Hydrochloride Tablet
Product Images NDC 63629-1930

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Oxycodone Hydrochloride (NDC 63629-1930). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bryant Ranch Prepack, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Fig1

Fig1
The text describes a figure, specifically "Figure 1" of a study that evaluates the dose-proportionality of oxycodone. The figure displays different doses, 0mg and 15mg, and is potentially related to a single-dose administration.*
FDA Label Image

Struct

FDA Label Image

Tab2

Tab2
The text presents pharmacokinetic parameters for different forms and doses of Oxycodone Hydrochloride, including data on AUC, concentration, and half-life under various conditions such as single and multiple doses, and with or without food. The text also includes mean and standard deviation values for these parameters.*
FDA Label Image

Label (Lbl636291930)

Label (Lbl636291930)
This is a description of a medication called NILD which contains oxycodone hydrochloride in the strength of 30 mg per tablet. It is advised to keep this medication away from children and store it at a temperature between 20°C to 25°C. It must be kept in a tightly sealed container with a child-resistant closure to prevent accidents. The medication may cause addiction and overdose, hence extra caution is advised while handling it. This medicine comes in a pack of 500 tablets and is available only with a doctor's prescription.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.